Enterprise HL7 / FHIR Terminology Engine
Universal Clinical Codes & Terminology Search
Search, verify, and inspect standardized LOINC, SNOMED CT, ICD-10-CM, RxNorm, and CPT clinical codes with native HL7 FHIR R4 resource mappings.
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| Code Value | Display Description | Code System & OID | FHIR Resource | Category | Status | Actions |
|---|---|---|---|---|---|---|
|
0272U
|
Hematology (genetic bleeding disorders) genomic sequence analysis of 51 genes blood buccal swab or amniotic fluid comprehensive
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0273T
|
Interrogation device evaluation (in person) carotid sinus baroreflex activation system including telemetric iterative communication with the implantable device to monitor device diagnostics and programmed therapy values with interpretation and report (eg battery status lead impedance pulse amplitude pulse width therapy frequency pathway mode burst mode therapy start/stop times each day); with programming
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0273U
|
Hematology (genetic hyperfibrinolysis delayed bleeding) analysis of 9 genes (F13A1 F13B FGA FGB FGG SERPINA1 SERPINE1 SERPINF2 by next-generation sequencing and PLAU by array comparative genomic hybridization) blood buccal swab or amniotic fluid
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0274T
|
Percutaneous laminotomy/laminectomy (interlaminar approach) for decompression of neural elements (with or without ligamentous resection discectomy facetectomy and/or foraminotomy) any method under indirect image guidance (eg fluoroscopic CT) with or without the use of an endoscope single or multiple levels unilateral or bilateral; cervical or thoracic
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0274U
|
Hematology (genetic platelet disorders) genomic sequence analysis of 43 genes blood buccal swab or amniotic fluid
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0275T
|
Percutaneous laminotomy/laminectomy (interlaminar approach) for decompression of neural elements (with or without ligamentous resection discectomy facetectomy and/or foraminotomy) any method under indirect image guidance (eg fluoroscopic CT) with or without the use of an endoscope single or multiple levels unilateral or bilateral; lumbar
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0275U
|
Hematology (heparin-induced thrombocytopenia) platelet antibody reactivity by flow cytometry serum
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0276T
|
Bronchoscopy rigid or flexible including fluoroscopic guidance when performed; with bronchial thermoplasty 1 lobe
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0276U
|
Hematology (inherited thrombocytopenia) genomic sequence analysis of 42 genes blood buccal swab or amniotic fluid
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0277T
|
Bronchoscopy rigid or flexible including fluoroscopic guidance when performed; with bronchial thermoplasty 2 or more lobes
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0277U
|
Hematology (genetic platelet function disorder) genomic sequence analysis of 31 genes blood buccal swab or amniotic fluid
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0278T
|
Transcutaneous electrical modulation pain reprocessing (eg scrambler therapy) each treatment session (includes placement of electrodes)
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0278U
|
Hematology (genetic thrombosis) genomic sequence analysis of 12 genes blood buccal swab or amniotic fluid
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0279T
|
Cell enumeration using immunologic selection and identification in fluid specimen (eg circulating tumor cells in blood);
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0279U
|
Hematology (von Willebrand disease [VWD]) von Willebrand factor (VWF) and collagen III binding by enzyme-linked immunosorbent assays (ELISA) plasma report of collagen III binding
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0280T
|
Cell enumeration using immunologic selection and identification in fluid specimen (eg circulating tumor cells in blood); interpretation and report
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0280U
|
Hematology (von Willebrand disease [VWD]) von Willebrand factor (VWF) and collagen IV binding by enzyme-linked immunosorbent assays (ELISA) plasma report of collagen IV binding
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0281T
|
Percutaneous transcatheter closure of the left atrial appendage with implant including fluoroscopy transseptal puncture catheter placement(s) left atrial angiography left atrial appendage angiography radiological supervision and interpretation
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0281U
|
Hematology (von Willebrand disease [VWD]) von Willebrand propeptide enzyme-linked immunosorbent assays (ELISA) plasma diagnostic report of von Willebrand factor (VWF) propeptide antigen level
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
|
0282T
|
Percutaneous or open implantation of neurostimulator electrode array(s) subcutaneous (peripheral subcutaneous field stimulation) including imaging guidance when performed cervical thoracic or lumbar; for trial including removal at the conclusion of trial period
|
CPT
2.16.840.1.113883.6.12
|
Procedures | Procedures | Active |
|
Healthcare Terminology & FHIR R4 Interoperability
Standardized coding guidelines governed by CodesForMD
In HL7 FHIR R4, discrete clinical findings and laboratory measurements are encapsulated inside
Observation resources. Diagnostic terms and problem list entries are represented within Condition resources, while surgical and therapeutic acts map to Procedure. CodesForMD adheres to official US Core and International FHIR Implementation Guides.
An OID is an internationally standardized dotted-decimal identifier (e.g.
2.16.840.1.113883.6.1 for LOINC) registered with HL7 and ISO. OIDs ensure unambiguous identification of terminology authorities when exchanging clinical messages across heterogeneous EHR, LIS, and PACS systems.
Yes. You can visit our platform's administrative ingestion and export engine or contact our team to obtain batch files of standardized codes.